Canonical Allele Identifier: CA276958369
Community Standard Title: NM_032444.4(SLX4):c.4283G>A (p.Trp1428Ter)
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3589355C>T , CM000678.2:g.3589355C>T GRCh38
NC_000016.9:g.3639356C>T , CM000678.1:g.3639356C>T GRCh37
NC_000016.8:g.3579357C>T NCBI36
NG_028123.1:g.27230G>A , LRG_503:g.27230G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.4283G>A MANE Select NP_115820.2:p.Trp1428Ter
ENST00000294008.4:c.4283G>A MANE Select ENSP00000294008.3:p.Trp1428Ter
NM_032444.2:c.4283G>A , LRG_503t1:c.4283G>A NP_115820.2:p.Trp1428Ter
NM_032444.3:c.4283G>A NP_115820.2:p.Trp1428Ter
ENST00000294008.3:c.4283G>A ENSP00000294008.3:p.Trp1428Ter
XM_011522715.1:c.4283G>A XP_011521017.1:p.Trp1428Ter
XM_011522715.3:c.4283G>A XP_011521017.1:p.Trp1428Ter
XM_017023775.2:c.3461G>A XP_016879264.1:p.Trp1154Ter
XM_024450471.1:c.4283G>A XP_024306239.1:p.Trp1428Ter